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HRID 12886作成日:2026年10月26日
2-Propenoic acid, 2-cyano-3-ethoxy-, ethyl ester → ethyl 5-amino-1-cyclopentyl-1H-pyrazole-4-carboxylate
https://huagongshe.com/reaction/12886
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 2-Propenoic acid, 2-cyano-3-ethoxy-, ethyl ester | HCID 78943 | — |
| 反応物 | Cyclopentylhydrazine hydrochloride | HCID 212349 | — |
| 反応物 | Sodium Acetate | HCID 517045 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | ethyl 5-amino-1-cyclopentyl-1H-pyrazole-4-carboxylate | HCID 12508126 | 79.3% |
反応手順
Cyclopentyl-hydrazine hydrochloride (1.000 g; 7.32 mmol), ethyl (ethoxymethylene)-cyanoacetate (1.026 g, 6.61 mmol) and anhydrous sodium acetate (0.644 g, 7.85 mmol) were combined in ethanol (10 mL) and heated at 70° C. for 20 hours. After cooling to room temperature, ethanol was removed in vacuo and the residue was partitioned between methylene chloride and water. The organic phase was washed sequentially with water and brine. Each aqueous phase was back extracted with a single portion of methylene chloride. The two organic phases were combined, dried over sodium sulfate and concentrated. Purification by flash chromatography, eluting with 10-40% EtOAc/hexanes yielded 5-amino-1-cyclopentyl-1H-pyrazole-4-carboxylic acid ethyl ester (1.170 g, 73%). Mass spectrum: m/z: 224.1 (M+H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07728029B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-660058880d6144ccbdfae5625f97875b |
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| 出典メモ | uspto-grants-2010_06 |
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